| NDC Code | 52125-617-17 |
|---|
| Package Description | 4 TABLET, FILM COATED in 1 BOTTLE (52125-617-17) |
|---|
| Product NDC | 52125-617 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Valacyclovir Hydrochloride |
|---|
| Non-Proprietary Name | Valacyclovir Hydrochloride |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20130405 |
|---|
| End Marketing Date | 20170823 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA090370 |
|---|
| Manufacturer | REMEDYREPACK INC. |
|---|
| Substance Name | VALACYCLOVIR HYDROCHLORIDE |
|---|
| Strength | 1 |
|---|
| Strength Unit | g/1 |
|---|
| Pharmacy Classes | DNA Polymerase Inhibitors [MoA],Herpes Simplex Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC],Herpes Zoster Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC],Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor [EPC],Nucleoside Analog [Chemical/Ingredient] |
|---|